Valsartan

Product NDC
72189-550
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Valsartan
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Direct_Rx
Application
ANDA205536
Marketing category
ANDA
Substance
VALSARTAN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72189-550-3030 TABLET, FILM COATED in 1 BOTTLE (72189-550-30) 2024-04-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ValsartanDirect_Rx2024-04-26HUMAN PRESCRIPTION DRUG LABEL1